I am an analytical and results-oriented professional with +4 years experience in regulatory affairs and quality management for medical devices manufacturers. I have developed and implemented quality management systems in order to obtain Good Manufacturing Practice certificates. Also, designed and typed quality manuals, standard operating procedures, documents, files and KPIs, as well as electromedical equipments User's manuals, brochures, dossiers, risk and usability files.
+3 years experience in research and developments of different medical devices and services.
Advance knowledge in Office package, Matlab, C++.